Tehničko veleučilište u Zagrebu · Zagreb

Do IL-1B and IL-1RN modulate chronic low back pain in patients with post-traumatic stress disorder?

izvorni znanstveni rad

izvorni znanstveni rad

Do IL-1B and IL-1RN modulate chronic low back pain in patients with post-traumatic stress disorder?

Vrsta prilog u časopisu
Tip izvorni znanstveni rad
Godina 2013
Časopis Collegium antropologicum
Nadređena publikacija Collegium antropologicum
Volumen 37
Svesčić 4
Stranice str. 1237-1244
ISSN 0350-6134
EISSN 1848-9486
Status objavljeno

Sažetak

The aim of this study was to analyze association between single nucleotide polymorphism (SNP) in IL1B (rs1143634) and IL1RN (rs 2234677) with chronic low back pain (LBP) in chronic post-traumatic stress disorder (PTSD). A total of 406 war veterans from 1991- 1995 war in Croatia participated in this study. They were divided into four groups, according to psychiatric interview, psychometric testing and the presence of LBP, verified by the imaging lumbar area, into: (i) war veterans suffering from PTSD and LBP (N=102), (ii) war veterans suffering from PTSD only (N=108), (iii) war veterans suffering from LBP only (N=99), (iv) healthy controls (N=97). Each subject provided blood sample for IL1B and IL1RN polymorphism testing. We found no association of rs1143634 in IL1-B with LBP. Permutation test showed significant association of rs 1143634 in IL1-RN with LBP group and presence of wild type allele A was protective in LBP group. The same SNP (rs1143634) in IL1-B was associated with the intensity of pain. No other associations were observed between these two markers and self-reported measures evaluating PTSD and pain symptoms. These results suggest potential role of cytokine network in the pathogenesis of chronic PTSD and LBP, although the direct causative pathway remains unclear. The alterations of cytokine network on the level of the brain, spinal medulla and the spine may be responsible for modulation of pain and occurrence of LBP.

Ključne riječi

PTSD ; chronic pain ; single nucleotide polymorphism ; IL-1B ; IL-1RN